FDA found Listeria Monocytogenes in Bleating Heart Cheese's Moolicious Blue blue cheese. Recalled products were made between Feb 14 and Sept 19, 2014. Consumers should check labels for codes 14-0214 to 14-0919.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
Bleating Heart Cheese is recalling its Moolicious Blue blue cheese due to Listeria Monocytogenes contamination found in FDA samples. This poses a risk of serious illness, so affected consumers should stop using the product immediately.
Listeria Monocytogenes is a bacterium that can cause severe food poisoning, especially in pregnant women, newborns, and people with weakened immune systems. FDA samples detected this bacteria in three varieties of the cheese.
Consumers who purchased Bleating Heart Cheese Moolicious Blue blue cheese between February 14 and September 19, 2014 are affected. Those with compromised immune systems are at higher risk for serious illness.
Check the product label for the code on the package, which ranges from 14-0214 to 14-0919. The cheese was produced between February 14 and September 19, 2014.
Immediately discard any Bleating Heart Cheese Moolicious Blue blue cheese with codes 14-0214 to 14-0919.
No, FDA samples found Listeria Monocytogenes in this cheese, which can cause serious illness. Do not consume.
The cheese was produced between February 14, 2014 (coded 14-0214) and September 19, 2014 (coded 14-0919).
Check the product label for the code on the package. If it shows a code between 14-0214 and 14-0919, it is recalled.
We’ve drafted a message you can send Bleating Heart Cheese to request your refund or repair — edit it as you like.
Subject: Recall F-0954-2015 — Bleating Heart Cheese Bleating Heart Cheese Hello, I own a Bleating Heart Cheese that is covered by recall F-0954-2015 from Bleating Heart Cheese. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
